EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test
Genetic testing is an important tool in the diagnosis and management of various genetic disorders. One such disorder is Leukoencephalopathy with vanishing white matter (VWM), which is associated with mutations in the EIF2B4 gene.
VWM is a progressive neurological disorder that affects the brain’s white matter, leading to a loss of myelin, the protective covering around nerve fibers. To diagnose this condition, a genetic test specifically targeting the EIF2B4 gene can be performed.
Test Details
The EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test is a comprehensive analysis of the DNA sequence of the EIF2B4 gene. This test utilizes NGS (Next-Generation Sequencing) technology to identify any mutations or variations in the gene that may be causing or predisposing an individual to VWM.
Test Components and Price
The cost of the EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test is AED 4400.0. The test can be performed using a blood sample, extracted DNA, or one drop of blood on an FTA card.
Test Type and Doctor
The EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test falls under the category of Neurological Disorders. It is recommended to consult with a Neurologist for this test.
Test Department and Pre Test Information
The test is conducted in the Genetics department. Before undergoing the EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be required to draw a pedigree chart of family members affected by VWM.
Report Delivery and Method
The report for the EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test is typically delivered within 3 to 4 weeks. The test utilizes NGS technology for accurate and comprehensive analysis of the EIF2B4 gene.
Importance of Genetic Testing for VWM
Genetic testing for VWM is a crucial step in the diagnosis and management of this progressive neurological disorder. It provides valuable information for genetic counseling and can potentially guide treatment decisions. However, it is important to undergo genetic testing under the guidance of a healthcare professional, such as a Neurologist, genetic counselor, or medical geneticist. These professionals can interpret the test results and provide appropriate recommendations and support.
| Test Name | EIF2B4 Gene Leukoencephalopathy with vanishing white matter Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for EIF2B4 Gene Leukoencephalopathy with vanishing white matter NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with EIF2B4 Gene Leukoencephalopathy with vanishing white matter |
| Test Details | The EIF2B4 gene is associated with a genetic disorder called Leukoencephalopathy with vanishing white matter (VWM). VWM is a progressive neurological disorder that affects the brain’s white matter, leading to a loss of myelin, which is the protective covering around nerve fibers. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the EIF2B4 gene to identify any mutations or variations that may be causing or predisposing an individual to VWM. This type of genetic testing can help with diagnosis, genetic counseling, and potentially guide treatment decisions. It is important to note that genetic testing for VWM should be done under the guidance of a healthcare professional, such as a genetic counselor or a medical geneticist, who can interpret the results and provide appropriate recommendations and support. |
